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scopus: 7102600487

Seeger, J.

(Jürgen Seeger)


patient tyrosine hydroxylase mutation tyrosine hydroxylase month l-dopa ficiency dystonia erasmus university rotterdam type b patients disorder .698g tyrosine hydroxylase gene university brain dopamine onset treatment department table hva /5hiaa ratio phenotype feature concentration rondot hoffmann diagnosis analysis response neurology brautigam wever paediatric movement children effect verbeek l-dopa-responsive reference protein hospital erasmu wevers ra b patients rotterdam 1810–1822 literature biosynthesi downloaded nijmegen allele ratio centre rijk-van andel extrapyramidal movement disorder .707t steenbergen-spanjers gc /5hiaa rijk-van andel jf heuvel syndrome netherland neurotransmitter family willemsen andel muller .à70g rijk-van hypokinetic-rigid syndrome thd patients mutation analysis study genet hoffmann gf paediatric neurology missense mutations l-dopa-responsive dystonia tyrosine hydroxylase activity




1 Most Recent Publications

Tyrosine hydroxylase deficiency: A treatable disorder of brain catecholamine biosynthesis (Article)
Willemsen, M.A. Verbeek, M.M. Haeussler, M. Hoffmann, G.F. Jung, H. Klerk, J.B.C. de Knaap, M.S. van der Kok, F. Leuzzi, V. Lonlay, P. de Megarbane, A. Monaghan, H. Kamsteeg, E.J. Renier, W.O. Rondot, P. Ryan, M.M. Seeger, J. Smeitink, J.A.M. Steenbergen-Spanjers, G.C. Wassmer, E. Weschke, B. Wijburg, F.A. Wilcken, B. Rijk-Van Andel, J.F. de Zafeiriou, D.I. Wevers, R.A. Aeby, A. Blau, N. Burlina, A.B. Donati, M.A. Geurtz, B. Grattan-Smith, P.J.
2010-06-01